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KNEE QD COIL MRT 50A

Page Type
Cleared 510(K)
510(k) Number
K902316
510(k) Type
Traditional
Applicant
TOSHIBA AMERICA MRI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/1990
Days to Decision
70 days

KNEE QD COIL MRT 50A

Page Type
Cleared 510(K)
510(k) Number
K902316
510(k) Type
Traditional
Applicant
TOSHIBA AMERICA MRI, INC.
Country
United States
FDA Decision
Substantially Equivalent
Decision Date
8/1/1990
Days to Decision
70 days